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Associate Researcher

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Research Associate
Location: Manchester, UK
Work Setting: Site-based / UK travel
Employment Type: Full-time
Industry: Clinical Research / Life Sciences
Function: Clinical Operations / Research
Visa Sponsorship: Not available
About the Role
An international clinical research organisation is seeking a Research Associate to support Oncology clinical trials across UK sites. The role involves independent site monitoring and close collaboration with investigators and study teams throughout the trial lifecycle.
Reasons to use Rodeo
I’m in my final year doing Economics and I don’t know whether to apply for grad schemes now or do a masters first. What do you think?
Honest answer — it depends on where you want to end up. A lot of top grad schemes (Big 4, civil service, banking) don’t need a masters. Let’s look at the ones you’d be competitive for now, and we can decide if a masters actually adds anything.
Also worth knowing: most autumn 2026 applications are open now. Timing matters more than you think.
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Graduate Consultant — 2026 Scheme
Why you're a good match
StrongYour economics background and your summer at a regional bank line up with what PwC looks for on the consulting scheme. Applications close in four weeks.
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Why you're a good match
You’ve got the grades and the economics background, and your bank internship is exactly the experience this scheme looks for. Apply soon — deadlines close within the month.
Experience fit
Your summer at the bank plus your econometrics coursework map directly to the day-one responsibilities on this scheme — client modelling, market briefings, and deal support.
Only hits
No noise. No "maybe this fits." Just roles with a clear explanation of why they're right — and where to focus when applying.
Key Responsibilities
- Conduct site selection, initiation, monitoring, and close-out visits in line with GCP.
- Support site recruitment plans and study delivery.
- Provide protocol and study training to assigned sites.
- Monitor site quality, data integrity, and regulatory compliance.
- Track regulatory submissions, recruitment, CRF completion, and data queries.
- Maintain TMF/ISF documentation in accordance with GCP requirements.
- Document monitoring findings, action plans, and follow-up activities.
- Collaborate with study teams and sites to resolve issues and maintain project progress.


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Requirements
- Experience conducting independent on-site monitoring in Oncology, preferably on unblinded studies.
- Strong knowledge of GCP and ICH guidelines.
- Life science degree or equivalent clinical research industry experience.
- Willingness and flexibility to travel to UK sites.
Note: This position is not eligible for visa sponsorship.
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Jessica, London